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Potentially repurposable drugs for COVID-19 identified from SARS-CoV-2 Host Protein Interactome
We previously presented the protein-protein interaction network - the ‘HoP’ or the host protein interactome - of 332 host proteins that were identified to interact with 27 nCoV19 viral proteins by Gordon et al. Here, we studied drugs targeting the proteins in this interactome to identify whether any...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Journal Experts
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7336709/ https://www.ncbi.nlm.nih.gov/pubmed/32702734 http://dx.doi.org/10.21203/rs.3.rs-30363/v1 |
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author | Karunakaran, Kalyani B. Balakrishnan, N. Ganapathiraju, Madhavi |
author_facet | Karunakaran, Kalyani B. Balakrishnan, N. Ganapathiraju, Madhavi |
author_sort | Karunakaran, Kalyani B. |
collection | PubMed |
description | We previously presented the protein-protein interaction network - the ‘HoP’ or the host protein interactome - of 332 host proteins that were identified to interact with 27 nCoV19 viral proteins by Gordon et al. Here, we studied drugs targeting the proteins in this interactome to identify whether any of them may potentially be repurposable against SARS-CoV-2. We studied each of the drugs using the BaseSpace Correlation Engine and identified those that induce gene expression profiles negatively correlated with SARS-associated expression profile. This analysis resulted in 20 drugs whose differential gene expression (drug versus normal) had an anti-correlation with differential expression for SARS (viral infection versus normal). These included drugs that were already being tested for their clinical activity against SARS-CoV-2, those with proven activity against SARS-CoV/MERS-CoV, broad-spectrum antiviral drugs, and those identified/prioritized by other computational re-purposing studies. In summary, our integrated computational analysis of the HoP interactome in conjunction with drug-induced transcriptomic data resulted in drugs that may be repurposable for COVID-19. |
format | Online Article Text |
id | pubmed-7336709 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Journal Experts |
record_format | MEDLINE/PubMed |
spelling | pubmed-73367092020-07-14 Potentially repurposable drugs for COVID-19 identified from SARS-CoV-2 Host Protein Interactome Karunakaran, Kalyani B. Balakrishnan, N. Ganapathiraju, Madhavi Res Sq Article We previously presented the protein-protein interaction network - the ‘HoP’ or the host protein interactome - of 332 host proteins that were identified to interact with 27 nCoV19 viral proteins by Gordon et al. Here, we studied drugs targeting the proteins in this interactome to identify whether any of them may potentially be repurposable against SARS-CoV-2. We studied each of the drugs using the BaseSpace Correlation Engine and identified those that induce gene expression profiles negatively correlated with SARS-associated expression profile. This analysis resulted in 20 drugs whose differential gene expression (drug versus normal) had an anti-correlation with differential expression for SARS (viral infection versus normal). These included drugs that were already being tested for their clinical activity against SARS-CoV-2, those with proven activity against SARS-CoV/MERS-CoV, broad-spectrum antiviral drugs, and those identified/prioritized by other computational re-purposing studies. In summary, our integrated computational analysis of the HoP interactome in conjunction with drug-induced transcriptomic data resulted in drugs that may be repurposable for COVID-19. American Journal Experts 2020-05-28 /pmc/articles/PMC7336709/ /pubmed/32702734 http://dx.doi.org/10.21203/rs.3.rs-30363/v1 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Karunakaran, Kalyani B. Balakrishnan, N. Ganapathiraju, Madhavi Potentially repurposable drugs for COVID-19 identified from SARS-CoV-2 Host Protein Interactome |
title | Potentially repurposable drugs for COVID-19 identified from SARS-CoV-2 Host Protein Interactome |
title_full | Potentially repurposable drugs for COVID-19 identified from SARS-CoV-2 Host Protein Interactome |
title_fullStr | Potentially repurposable drugs for COVID-19 identified from SARS-CoV-2 Host Protein Interactome |
title_full_unstemmed | Potentially repurposable drugs for COVID-19 identified from SARS-CoV-2 Host Protein Interactome |
title_short | Potentially repurposable drugs for COVID-19 identified from SARS-CoV-2 Host Protein Interactome |
title_sort | potentially repurposable drugs for covid-19 identified from sars-cov-2 host protein interactome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7336709/ https://www.ncbi.nlm.nih.gov/pubmed/32702734 http://dx.doi.org/10.21203/rs.3.rs-30363/v1 |
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